Identity
- Trade Name
- Good Sense FDA UDI
- Generic Name
- Multi-purpose soft contact lens solution FDA UDI
- Device Name
- GOODSENSE MULTI-PURPOSE SOLUTION 12 OZ FDA UDI
- Model / Reference
- KC00960 FDA UDI
- Description
- GOODSENSE MULTI-PURPOSE SOLUTION 12 OZ FDA UDI
Identifiers
- Catalog Number
- 9MPSA1201GSGS FDA UDI
- Primary DI / UDI-DI
- 00846036009606 FDA UDI
- FDA Product Code
- LYL FDA UDI
- GMDN Term
- Multi-purpose soft contact lens solution FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5928 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multi-purpose soft contact lens solution
Good Sense by Geiss, Destin & Dunn, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Geiss, Destin & Dunn, Inc
Sources (1)
- FDA UDI ace45291-4987-43fb-b1a2-3af1cafbc3ca 35 fields · synced May 30, 2026